Hand Sanitizer

Manufacturer
Saint Medicine Inc. | Guangzhou Zhongkebaishi Health Industry CO., LTD
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:25:42

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Pump a small amount of gel into palm of hand Rub thoroughly over all surfaces of both bands Rub hands together briskly until dry

Storage and handling

Keep away from the direct sunlight Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of gel into palm of hand

Rub thoroughly over all surfaces of both bands

Rub hands together briskly until dry

Other information

STORAGE AND HANDLING SECTION

Keep away from the direct sunlight

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Aloe Barbadense Leaf Extract, Carbomer, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

480 mL NDC: 72784-351-91

PDPPDP

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72784-35172784-351-91
73813-2011

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bae2333f-8655-1c8b-e053-2a95a90a74b0a4a3e971-3b98-0c05-e053-2a95a90a20fc2021-02-09WarningsExact identifier
spl set id: a4a3e971-3b98-0c05-e053-2a95a90a20fc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.